Studies of the Molecular Recognition Abilities of Gallic Acid-Imprinted Polymer Prepared Using a Molecular Imprinting Technique

The present work compares the molecular recognition abilities of two molecularly imprinted polymers (MIPs) synthesized using two different functional monomers, viz. acrylamide (AA) and 4-vinylpyridine (4-Vp), employing gallic acid (GA) as the template using the non-covalent imprinting approach emplo...

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Main Authors: Sushma Pardeshi, Rita Dhodapkar, Anupama Kumar
Format: Article
Language:English
Published: Hindawi - SAGE Publishing 2012-01-01
Series:Adsorption Science & Technology
Online Access:https://doi.org/10.1260/0263-6174.30.1.23
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spelling doaj-2991e8ea4b234e85a7d4b43dab4955a52021-04-02T18:20:11ZengHindawi - SAGE PublishingAdsorption Science & Technology0263-61742048-40382012-01-013010.1260/0263-6174.30.1.23Studies of the Molecular Recognition Abilities of Gallic Acid-Imprinted Polymer Prepared Using a Molecular Imprinting TechniqueSushma Pardeshi0Rita Dhodapkar1Anupama Kumar2 Chemistry Department, Visvesvaraya National Institute of Technology, Nagpur, 440010 (M.S.), India Waste Water Technology Division, National Environmental Engineering Research Institute, CSIR, Nagpur, 440020 (M.S.), India Chemistry Department, Visvesvaraya National Institute of Technology, Nagpur, 440010 (M.S.), IndiaThe present work compares the molecular recognition abilities of two molecularly imprinted polymers (MIPs) synthesized using two different functional monomers, viz. acrylamide (AA) and 4-vinylpyridine (4-Vp), employing gallic acid (GA) as the template using the non-covalent imprinting approach employing ethylene glycol dimethacrylate (EGDMA) as the cross-linker and 2,2-azo-bis-2-isobutyronitrile (AIBN) as an initiator in the porogen acetonitrile by thermal polymerization. The change in the electronic stabilization energies (ΔE) of the template–monomer complexes formed between the template and functional monomers in the presence of the porogen were computed using Density Functional Theory (DFT) to interpret the nature of the interactions between them and to compare their stabilities. A systematic investigation of the molecular recognition abilities of the synthesized MIPs has been carried out by applying the Langmuir–Freundlich (L–F) adsorption isotherm model. The binding parameters obtained from the L–F model demonstrate that MIP AA exhibited a higher specific molecular recognition ability towards the template molecule.https://doi.org/10.1260/0263-6174.30.1.23
collection DOAJ
language English
format Article
sources DOAJ
author Sushma Pardeshi
Rita Dhodapkar
Anupama Kumar
spellingShingle Sushma Pardeshi
Rita Dhodapkar
Anupama Kumar
Studies of the Molecular Recognition Abilities of Gallic Acid-Imprinted Polymer Prepared Using a Molecular Imprinting Technique
Adsorption Science & Technology
author_facet Sushma Pardeshi
Rita Dhodapkar
Anupama Kumar
author_sort Sushma Pardeshi
title Studies of the Molecular Recognition Abilities of Gallic Acid-Imprinted Polymer Prepared Using a Molecular Imprinting Technique
title_short Studies of the Molecular Recognition Abilities of Gallic Acid-Imprinted Polymer Prepared Using a Molecular Imprinting Technique
title_full Studies of the Molecular Recognition Abilities of Gallic Acid-Imprinted Polymer Prepared Using a Molecular Imprinting Technique
title_fullStr Studies of the Molecular Recognition Abilities of Gallic Acid-Imprinted Polymer Prepared Using a Molecular Imprinting Technique
title_full_unstemmed Studies of the Molecular Recognition Abilities of Gallic Acid-Imprinted Polymer Prepared Using a Molecular Imprinting Technique
title_sort studies of the molecular recognition abilities of gallic acid-imprinted polymer prepared using a molecular imprinting technique
publisher Hindawi - SAGE Publishing
series Adsorption Science & Technology
issn 0263-6174
2048-4038
publishDate 2012-01-01
description The present work compares the molecular recognition abilities of two molecularly imprinted polymers (MIPs) synthesized using two different functional monomers, viz. acrylamide (AA) and 4-vinylpyridine (4-Vp), employing gallic acid (GA) as the template using the non-covalent imprinting approach employing ethylene glycol dimethacrylate (EGDMA) as the cross-linker and 2,2-azo-bis-2-isobutyronitrile (AIBN) as an initiator in the porogen acetonitrile by thermal polymerization. The change in the electronic stabilization energies (ΔE) of the template–monomer complexes formed between the template and functional monomers in the presence of the porogen were computed using Density Functional Theory (DFT) to interpret the nature of the interactions between them and to compare their stabilities. A systematic investigation of the molecular recognition abilities of the synthesized MIPs has been carried out by applying the Langmuir–Freundlich (L–F) adsorption isotherm model. The binding parameters obtained from the L–F model demonstrate that MIP AA exhibited a higher specific molecular recognition ability towards the template molecule.
url https://doi.org/10.1260/0263-6174.30.1.23
work_keys_str_mv AT sushmapardeshi studiesofthemolecularrecognitionabilitiesofgallicacidimprintedpolymerpreparedusingamolecularimprintingtechnique
AT ritadhodapkar studiesofthemolecularrecognitionabilitiesofgallicacidimprintedpolymerpreparedusingamolecularimprintingtechnique
AT anupamakumar studiesofthemolecularrecognitionabilitiesofgallicacidimprintedpolymerpreparedusingamolecularimprintingtechnique
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